BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 24009674)

  • 1. Exome sequencing and functional analysis identifies a novel mutation in EXT1 gene that causes multiple osteochondromas.
    Zhang F; Liang J; Guo X; Zhang Y; Wen Y; Li Q; Zhang Z; Ma W; Dai L; Liu X; Yang L; Wang J
    PLoS One; 2013; 8(8):e72316. PubMed ID: 24009674
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of a novel mutation in the EXT1 gene from a patient with multiple osteochondromas by exome sequencing.
    Hong G; Guo X; Yan W; Li Q; Zhao H; Ma P; Hu X
    Mol Med Rep; 2017 Feb; 15(2):657-664. PubMed ID: 28035357
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of Novel EXT Mutations in Patients with Hereditary Multiple Exostoses Using Whole-Exome Sequencing.
    Liang C; Wang YJ; Wei YX; Dong Y; Zhang ZC
    Orthop Surg; 2020 Jun; 12(3):990-996. PubMed ID: 32293802
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel Mutations in Chinese Patients with Multiple Osteochondromas Identified Using Whole Exome Sequencing.
    Tong Y; Luo J; Zhang Y; Hong Z; Cao L; Chen X; Chen J; Bi Q
    Genet Test Mol Biomarkers; 2021 May; 25(5):361-367. PubMed ID: 34003695
    [No Abstract]   [Full Text] [Related]  

  • 5. Identification of Novel Mutations in the
    Tong Y; Zhang Y; Luo J; Hong Z; Chen X; Bi Q
    Genet Test Mol Biomarkers; 2021 Feb; 25(2):145-151. PubMed ID: 33596140
    [No Abstract]   [Full Text] [Related]  

  • 6. Identification of mutations in EXT1 and EXT2 genes in six Chinese families with multiple osteochondromas.
    Xu Y; Kang Q; Zhang Z
    Mol Med Rep; 2017 Oct; 16(4):5599-5605. PubMed ID: 28849184
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Identification of a novel EXT1 mutation in a pedigree affected with hereditary multiple exostosis].
    Lou G; Yang K; Qin L; Zhang Y; Wang H; Hou Q; He M; Liao S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Feb; 35(1):91-95. PubMed ID: 29419870
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Novel EXT1 Mutation Identified in a Family with Multiple Osteochondromas.
    Chen Z; Bi Q; Kong M; Chen Y
    Genet Test Mol Biomarkers; 2019 Apr; 23(4):251-254. PubMed ID: 29989442
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of a novel EXT1 mutation in patients with hereditary multiple exostosis by exome sequencing.
    Liu H; Wu S; Duan L; Zhu W; Zhang S; Hu X; Jia W; Yang G; Liu C; Li W; Yang L; Guo L; Lin Y; Wang Y; He M; Yang Z; He Y; Cai Z; Wang D
    Oncol Rep; 2015 Feb; 33(2):547-52. PubMed ID: 25421355
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutation screening for the EXT1 and EXT2 genes in Chinese patients with multiple osteochondromas.
    Kang QL; Xu J; Zhang Z; He JW; Fu WZ; Zhang ZL
    Arch Med Res; 2013 Oct; 44(7):542-8. PubMed ID: 24120389
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutation analysis and prenatal diagnosis of EXT1 gene mutations in Chinese patients with multiple osteochondromas.
    Zhu HY; Hu YL; Yang Y; Wu X; Zhu RF; Zhu XY; Duan HL; Zhang Y; Zhou JY
    Chin Med J (Engl); 2011 Oct; 124(19):3054-7. PubMed ID: 22040554
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel mutation of EXT2 identified in a large family with multiple osteochondromas.
    Chen XJ; Zhang H; Tan ZP; Hu W; Yang YF
    Mol Med Rep; 2016 Nov; 14(5):4687-4691. PubMed ID: 27748933
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Targeted Next-Generation Sequencing Newly Identifies Mutations in Exostosin-1 and Exostosin-2 Genes of Patients with Multiple Osteochondromas.
    Guo X; Lin M; Shi T; Yan W; Chen W
    Tohoku J Exp Med; 2017 Jul; 242(3):173-181. PubMed ID: 28690282
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of a novel EXT2 frameshift mutation in a family with hereditary multiple exostoses by whole-exome sequencing.
    Yang M; Xie H; Xu B; Xiang Q; Wang H; Hu T; Liu S
    J Clin Lab Anal; 2021 Sep; 35(9):e23968. PubMed ID: 34403521
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of a novel mutation in EXT2 in a fourth-generation Korean family with multiple osteochondromas and overview of mutation spectrum.
    Yang A; Kim J; Jang JH; Lee C; Lee JE; Cho SY; Jin DK
    Ann Hum Genet; 2019 May; 83(3):160-170. PubMed ID: 30730578
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel and recurrent mutations in the EXT1 and EXT2 genes in Chinese kindreds with multiple osteochondromas.
    Wu Y; Xing X; Xu S; Ma H; Cao L; Wang S; Luo Y
    J Orthop Res; 2013 Sep; 31(9):1492-9. PubMed ID: 23629877
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Large-scale mutational analysis in the EXT1 and EXT2 genes for Japanese patients with multiple osteochondromas.
    Ishimaru D; Gotoh M; Takayama S; Kosaki R; Matsumoto Y; Narimatsu H; Sato T; Kimata K; Akiyama H; Shimizu K; Matsumoto K
    BMC Genet; 2016 Mar; 17():52. PubMed ID: 26961984
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Novel mutation of Y271H in EXT1 gene causes multiple exostoses].
    Li W; Hu ZM; Xie ZG; He HB; Pan Q; Xia K; Xia JH
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Aug; 32(4):546-50. PubMed ID: 17767039
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of pathogenic mutations in 6 Chinese families with multiple exostoses by whole-exome sequencing and multiplex ligation-dependent probe amplification: Case series.
    Long X; Li Z; Huang Y; Zhang L; Lv W; Teng Y; Linpeng S; Liang D; Wu L
    Medicine (Baltimore); 2019 May; 98(20):e15692. PubMed ID: 31096510
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutations in the EXT1 and EXT2 genes in Spanish patients with multiple osteochondromas.
    Sarrión P; Sangorrin A; Urreizti R; Delgado A; Artuch R; Martorell L; Armstrong J; Anton J; Torner F; Vilaseca MA; Nevado J; Lapunzina P; Asteggiano CG; Balcells S; Grinberg D
    Sci Rep; 2013; 3():1346. PubMed ID: 23439489
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.